New Alzheimer's disease susceptibility locus on chromosome 10q

Combined transfacial and transcranial approach for tumours of the nose and paranasal sinuses with intracranial extension.

Nigerian journal of medicine : journal of the National Association of Resident Doctors of Nigeria·2011

Combined transfacial and transcranial approach for tumours of the nose and paranasal sinuses with intracranial extension.

Nigerian journal of medicine : journal of the National Association of Resident Doctors of Nigeria·2011

Altered expression and coregulation of dopamine signalling genes in schizophrenia and bipolar disorder.

Neuropathology and applied neurobiology·2010

Paraptosis: mediation by MAP kinases and inhibition by AIP-1/Alix.

Cell death and differentiation·2004

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.

Nature genetics·2001

Cloning and characterization of three novel genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: candidate genes for ALS2.

Genomics·2001

Genetic Testing Unveils a Novel Thrombospondin-1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79-Year-Old Woman.

Clinical genetics·2026

A Novel De Novo STAG1 Variant at the RAD21 Binding Interface Is Associated With Hypoglycemia, Recurrent Fever, Immunodeficiency and Features of Classical Cohesinopathies.

Clinical genetics·2026

Pathogenicity of NUSAP1 Variants Is Defined by NMD-Escape: Evidence From Two Novel Cases and Systematic Population-Based Variant Analysis.

Clinical genetics·2026

Biallelic ABCA13 Loss-of-Function Variants in a Child With Neurodevelopmental Delay: A Case Report.

Clinical genetics·2026

Variants in the Imprinted IGF2 Gene: A Review and Phasing of De Novo Variants Using Long-Read Sequencing.

Clinical genetics·2026

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Clinical genetics·2026

Leveraging multi-source observations for vertical PM2.5 estimation: A deep learning fusion model.

Journal of hazardous materials·2026

ALCAPA syndrome: a rare cause of sudden cardiac arrest in adulthood?-a case report.

Journal of medical case reports·2026

Stanford Type B aortic dissection following transradial coronary angiography in a patient with an aberrant right subclavian artery: a case report.

Frontiers in cardiovascular medicine·2026

Aryl radical addition-dehydrocyclization drives rapid polycyclic aromatic hydrocarbon growth.

Nature communications·2026

Enhancement of secondary organic aerosol formation from isoprene photooxidation by ammonia.

Journal of environmental sciences (China)·2026

Variability and ozone formation potential of ambient non-methane hydrocarbons in a tropical semi-arid atmosphere of northwest India.

Journal of environmental sciences (China)·2026

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New Alzheimer's disease susceptibility locus on chromosome 10q

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Combined transfacial and transcranial approach for tumours of the nose and paranasal sinuses with intracranial extension.

Combined transfacial and transcranial approach for tumours of the nose and paranasal sinuses with intracranial extension.

Altered expression and coregulation of dopamine signalling genes in schizophrenia and bipolar disorder.

Paraptosis: mediation by MAP kinases and inhibition by AIP-1/Alix.

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.

Cloning and characterization of three novel genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: candidate genes for ALS2.

Genetic Testing Unveils a Novel Thrombospondin-1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79-Year-Old Woman.

A Novel De Novo STAG1 Variant at the RAD21 Binding Interface Is Associated With Hypoglycemia, Recurrent Fever, Immunodeficiency and Features of Classical Cohesinopathies.

Pathogenicity of NUSAP1 Variants Is Defined by NMD-Escape: Evidence From Two Novel Cases and Systematic Population-Based Variant Analysis.

Biallelic ABCA13 Loss-of-Function Variants in a Child With Neurodevelopmental Delay: A Case Report.

Variants in the Imprinted IGF2 Gene: A Review and Phasing of De Novo Variants Using Long-Read Sequencing.

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

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Stanford Type B aortic dissection following transradial coronary angiography in a patient with an aberrant right subclavian artery: a case report.

Aryl radical addition-dehydrocyclization drives rapid polycyclic aromatic hydrocarbon growth.

Enhancement of secondary organic aerosol formation from isoprene photooxidation by ammonia.

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New Alzheimer's disease susceptibility locus on chromosome 10q

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